A newly developed method for assessing co-exposure to free dose combinations: a proof-of-concept study using antihypertensive medications in Danish registers

IF 3.4 3区 医学 Q2 GERIATRICS & GERONTOLOGY
Maria Antonietta Barbieri, Sidse Marie Neumann Nielsen, Andrea Rossi, Elena Olmastroni, Manuela Casula, Edoardo Spina, Maurizio Sessa
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Abstract

Background

Elevated blood pressure is a major risk factor for severe medical conditions. Adherence to antihypertensive medication, especially in free-dose combinations, poses a significant challenge. This study aims to develop a novel method for assessing co-exposure to free-dose antihypertensive medications using secondary data sources.

Methods

A register-based cohort study was conducted on individuals aged 65 years or older in Denmark who initiated antihypertensive therapy from 1996 to 2016 and followed for 730 days from the index date. A new method was developed to assess co-exposure to antihypertensive medications through redeemed prescriptions, treatment episodes, and overlapping medication events. The method's accuracy was evaluated using a random sample of 400 individuals.

Results

A total of 1,021,819 individuals were included in the study, with a mean age of 68.8 years, and 53.7% were women. The method achieved 100% accuracy in identifying co-exposure periods. During the early stage of the follow-up (0–180 days), 54.1% of individuals were co-exposed to at least two antihypertensive medications, while 37.5% were co-exposed during the late stage of the follow-up period (181–730 days). The most frequent antihypertensive combinations included bendroflumethiazide and potassium with either amlodipine or enalapril in the early (13.2% and 12.5% of patients, respectively) and late stages (16.9% and 15.0% of patients, respectively).

Conclusions

The newly developed method effectively assesses co-exposure to antihypertensive medications, overcoming previous limitations. The findings reveal common co-exposure combinations and evolving trends in antihypertensive medication use among older individuals, reflecting changes in clinical practice and guidelines over two decades.

新开发的自由剂量组合共同暴露评估方法:利用丹麦登记册中的降压药物进行概念验证研究
背景血压升高是导致严重疾病的主要风险因素。坚持服用降压药,尤其是自由剂量联合用药是一项重大挑战。本研究旨在利用二手数据源开发一种新型方法,用于评估自由剂量降压药物的共同暴露情况。方法对丹麦 65 岁或以上、1996 年至 2016 年期间开始接受降压治疗的患者进行了一项以登记为基础的队列研究,并从指数日期开始随访了 730 天。研究人员开发了一种新方法,通过兑换处方、治疗发作和重叠用药事件来评估降压药物的共同暴露。研究共纳入 1,021,819 人,平均年龄为 68.8 岁,53.7% 为女性。该方法识别共同暴露期的准确率达到 100%。在随访初期(0-180 天),54.1% 的人至少共同暴露于两种降压药物,而在随访后期(181-730 天),37.5% 的人共同暴露于两种降压药物。最常见的降压药组合包括苄氟噻嗪和钾与氨氯地平或依那普利,分别占早期(13.2%和12.5%的患者)和晚期(16.9%和15.0%的患者)的比例。研究结果揭示了常见的共同暴露组合以及老年人使用降压药的演变趋势,反映了二十年来临床实践和指南的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
5.00%
发文量
283
审稿时长
1 months
期刊介绍: Aging clinical and experimental research offers a multidisciplinary forum on the progressing field of gerontology and geriatrics. The areas covered by the journal include: biogerontology, neurosciences, epidemiology, clinical gerontology and geriatric assessment, social, economical and behavioral gerontology. “Aging clinical and experimental research” appears bimonthly and publishes review articles, original papers and case reports.
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